EP0279818B1 - Procedure for manufacturing catalyst components for polymerizing olefines - Google Patents

Procedure for manufacturing catalyst components for polymerizing olefines Download PDF

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Publication number
EP0279818B1
EP0279818B1 EP87904047A EP87904047A EP0279818B1 EP 0279818 B1 EP0279818 B1 EP 0279818B1 EP 87904047 A EP87904047 A EP 87904047A EP 87904047 A EP87904047 A EP 87904047A EP 0279818 B1 EP0279818 B1 EP 0279818B1
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EP
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Prior art keywords
aliphatic
aromatic
catalyst
compound
chamber
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Expired - Lifetime
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EP87904047A
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German (de)
English (en)
French (fr)
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EP0279818A1 (en
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Eero Iiskola
Jukka Koskinen
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Borealis Holding AS
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Neste Oyj
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S526/908—Containing catalyst of specified particle size
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S526/909—Polymerization characterized by particle size of product

Definitions

  • the present invention relates to a procedure for manufacturing catalyst components to be used in polymerizing olefines.
  • the invention relates to the manufacturing of catalyst and carrier components having spherical shape, for olefine-polymerizing catalysts.
  • Such catalysts typically comprise a magnesiumbased carrier substance which has been treated with a titanium halogen compound, and often also with an electron donor compound. Numerous methods have been worked out for manufacturing catalysts of this type, and a very great number of different compounds have been applied in order to modify said typical catalysts.
  • the catalysts have highest possible activity and thereby the required catalyst quantity is as small as possible. It is furthermore possible by the selection of catalyst to influence many other polymerisation characteristics.
  • Endeavours are frequently directed towards a result in which the products that are obtained would be in the form of even-sized, preferably spherical particles. This is reached, for instance, by the aid of using a catalyst carrier substance which occurs in the form of spherical particles of uniform quality.
  • emulsion oil method a melt of the carrier component is emulsified in a suitable oil, to be present therein in the form of spherical melt particles.
  • the carrier particles in the emulsion are then shock-solidified by adding the emulsion into a cold hydrocarbon fluid, where the particles solidify.
  • preparing the carrier substance requires a component which is not useful in the later steps of catalyst manufacturing and which implies the existence of purifying and recirculation apparatus to this purpose.
  • Another significant drawback is that this a charge process, in which the retention time is often prolonged, even up to several hours.
  • the spray drying method has some drawbacks which are partly associated with the quality of the carrier components obtained by the method and partly also with the process factors themselves.
  • a change of the chemicals composition takes place all the time as solvent, to begin with, evaporates from the solution and, thereafter, from the surfaces of the solid carrier particles.
  • the composition of the particles that are produced is not fully under control.
  • the continuous evaporation of solvent from the particles causes growth of the particles' surface area and finally leads to particles which are porous and non-uniform in quality, containing varying amounts of solvent. Porosity detracts from the mechanical durability of the catalyst components and also impairs the activity of the catalyst that is obtained and its morphological properties.
  • the procedure of the invention is generally characterized in that said magnesium compound, or a mixture of said magnesium compound and said electron donor compound, is sprayed in molten state into a chamber, or volume, which has been cooled to a temperature at which the catalyst component solidifies from said melt in the form of particles with generally spherical shape, without any substantial evaporation of components, whereafter said titanium halide treatment is carried out.
  • the composition of the carrier solution is constant all the time and no solvent evaporation takes place, as is the case in the spray drying process.
  • the particles that are produced are therefore uniform in quality and their structure is not porous as is that of particles produced by the spray drying method.
  • the composition of the particles can be adjusted to be as desired, and it is thus understood that the composition does not change during the manufacturing process. As a consequence, the particles are also more durable mechanically.
  • the formation of particles takes place at comparatively low temperatures, at which the chemicals and solvents that are used neither evaporate nor decompose. The process is also safe because it is not necessary to evaporate large quantities of solvent.
  • a significant additional advantage of the procedure of the invention is that with its aid it is possible, in one apparatus and in one step, to produce either exclusively spherical carrier particles or carrier particles which contain other active, or inert, substances needed in the catalyst, or even fully completed active catalyst components which are directly applicable in polymerizing olefines. This is not possible in the spray drying method of the prior art.
  • EP patent 044 735 discloses a process for spraying a composition of the formula M m X p TY.nZ, where M is preferably magnesium, X is a halogen, T is a transition metal, preferably titanium, Y is a halogen, and Z is an alcohol. Consequently, the composition to be sprayed is essentially distinguished from the composition used in the process of the present patent application in that it contains a transition metal compound and that titanium trichloride is used as the transition metal compound. In the process described in the EP patent it is expressly intended to avoid the titanium tetrachloride treatment normally used in the adding of a transition metal compound.
  • the procedure of the invention is suitable for manufacturing carrier components of magnesium chloride.
  • carrier and catalyst components which contain, in addition to the above-mentioned magnesium compounds, electron donor compounds such as normally used in this kind of catalysts as well as other auxiliary substances which may be required.
  • electron donor compounds such as normally used in this kind of catalysts as well as other auxiliary substances which may be required.
  • alcohols are advantageously used, for instance methanol or ethanol. It is only a prerequisite for using a donor that the donor when mixed with a solid magnesium compound on heating forms a melt which can be sprayed with the aid of a nozzle.
  • the electron donor may thus be selected from the group comprising aliphatic or aromatic carboxylic acids, aliphatic or aromatic alkyl esters of carboxylic acids, aliphatic or aromatic ketones, aliphatic and aromatic aldehydes, aliphatic and aromatic alcohols, aliphatic and aromatic acid halides, aliphatic and aromatic nitriles, aliphatic and aromatic amines, and aromatic phosphines.
  • a highly recommendable and frequently used electron donor is diisobutylphtalate, and a recommendable alcohol is ethanol.
  • the mixtured to be sprayed is prepared simply by melting the selected catalyst component or component mixture.
  • the melt is conducted into the spraying chamber with the aid of a pump or advantageously of a pressurized, inert fluid, for instance nitrogen.
  • the melt, or solution, of the carrier compound is sprayed into a cooled chamber at a temperature which at least equals the melting point of said carrier compound which is used, advantageously one approximately equal to the melting point.
  • Spherical particles are manufactured by conducting the melt with the aid of pressure to a nozzle located in the spraying chamber, this nozzle dispersing it into fine droplets. It is possible with the choice of nozzle size to influence the size and size distribution of the carrier particles which are produced in the process.
  • cold inert gas for instance nitrogen or air, is conducted through the bottom of the chamber upward from below, which rapidly cools the particles coming from the nozzle.
  • the cooling may be enhanced by spraying at the same time into the chamber a cold, inert hydrocarbon or another liquid fluid. It is not necessary to spray the cooling gas or cooling fluid into the chamber in countercurrent to the sprayed melt. It is also possible to spray cooling fluid with the current of the melt spray if in this way fast enough solidifying to solid particles is achievable. What is essential in the cooling event is that the cooling is so fast that the melt solidifies to solid state before it hits the walls of the apparatus and that no significant evaporation of the components contained in the carrier substance has time to take place.
  • the catalyst particles fall down on the bottom of the spraying chamber or to the layer of liquid accumulating there, wherefrom they can be removed through the lower part of the spraying chamber.
  • the inert gases escaping from the upper part may be carried through a cyclone in order to separate any small carrier particles which may have been entrained.
  • a carrier component can be manufactured in the procedure of the invention in that a mixture of magnesium and ethanol is heated in an autoclave, in a nitrogen atmosphere, at least to its melting point or preferably slightly higher. The melting point is essentially dependent on the ethanol quantity added.
  • Compressed nitrogen is used to supply the molten mixture into the cooling chamber with the aid of a nozzle, which disperses the melt into small droplets.
  • cold inert cooling gas such as nitrogen or air (e.g. -20 o C)
  • an inert cooling liquid e.g. heptane.
  • Solid carrier particles will then be formed which have a diameter on the order of 0-100 ⁇ m.
  • the carrier particles accumulating on the bottom of the chamber are removed for further treatment, which may for instance be treatment with an electron donor, or an activation treatment.
  • the carrier particles are at this time already at a suitable temperature for the next treatment.
  • the procedure of the invention further enables such carrier components to be manufactured in the same apparatus which contain the above-mentioned electron donor compounds.
  • the exemplary case described above may be modified so that the substance mixture which is sprayed into the chamber contains, in addition to the magnesium component and the ethanol component, an electron donor component.
  • the carrier particles which solidify in the chamber may then be carried directly to the next manufacturing step, that is, to activation, for instance to titanizing, in which the treatment is carried out with titanium tetrachloride.
  • other active components may be added to the carrier component.
  • the procedure of the invention may further be applied in manufacturing completed catalysts treated with titanium tetrachloride.
  • the ways above described may then be applied so that for cooling fluid is used, instead of an inert fluid, cold titanium tetrachloride, which may be sprayed against the melt spray coming from the nozzle.
  • cooling fluid instead of an inert fluid, cold titanium tetrachloride, which may be sprayed against the melt spray coming from the nozzle.
  • simultaneous solidification of the catalyst component to solid particles and activation of the catalyst component to a completed, active catalyst component will take place, the latter being directly usable for polymerizing, or subjectable to various additive treatments if required.
  • the cooling during the first activation step renders possible high activity of the catalyst because the efficient cooling prevents unfavourable temperature increase during the titanizing in the first step.
  • the invention is further illustrated by referring to the appended figure, which presents an apparatus appropriate for applying the procedure of the invention.
  • the apparatus 10 of the invention comprises a mixing tank 11 for mixing and melting the catalyst components and into which the catalyst components which are used, such as carrier component, alcohol or electron donors, can be introduced through the connector 12.
  • the mixing tank 11 may also be conducted inert, pressurized nitrogen gas through the pipe 13, and the mixing tank 11 has in addition been provided with a heating means 14 for melting the catalyst component mixture.
  • the mixture melted in the mixing tank 11 is conducted with the aid of nitrogen pressure by the heat-escorted pipe 15 to the spraying chamber 16, to the nozzle 17, where it is dispersed into small droplets.
  • Into the spraying chamber 16 is also conducted cold inert cooling gas by the nozzles 18 and cold liquid cooling fluid with the aid of the pipe 19 and nozzles 20.
  • the gases escape through the pipe 21 to a separator 22, where any solid catalyst components that may have been entrained can be removed.
  • the solidified catalyst particles are removed from the lower part of the chamber 16 by the pipe 23 to a product container 24, in which for instance the next treatment step may be carried out, which may for instance be treatment with an electron donor compound or activation, or additional activation.
  • a nitrogenated autoclave of capacity 110 litres was charged with 35 kg of dry MgCl2, 65 litres of dry EtOH and 10 litres of diisobutylphtalate. This reaction mix was melted at +110 o C, with mixing at the ultimate stage. After mixing for 2 hrs, the clear, homogenized mixture was supplied at a rate of 10 kg/h into a cooled spray chamber, into which nitrogen at -20 o C was conducted for cooling fluid.
  • the nozzle type was a 9-mm gas/liquid fluidizing nozzle with melt feeding aperture 1.0 mm in diameter and spraying angle 60 o . Dried nitrogen at +130 o C served as spraying gas, its feed rate being 1 kg/h.
  • the product was free-flowing and spherical in shape, and it emerged at temperature about 0 o C.
  • the analytic result was Mg 9.2% by wt. and Cl 26.3% by wt., according to which the chemical composition of the product was the same as that of the starting material melt: MgCl2 ⁇ 3 EtOH ⁇ 0.1 DIBP.
  • the particle size distribution was in the range 10-300 micra.
  • the fraction ⁇ 74 micra was separated from the product by screening, for activation of the catalyst carrier.
  • Preparation of carrier and catalyst was performed in a nitrogen atmosphere with H2O ⁇ 5 ppm and O2 ⁇ 5 ppm. Activation took place as follows, using TiCl4/EtOH mole ratio: 8.7: 27.2 g of the above, screened product were added at 0 o C into 300 ml of TiCl4.
  • the carrier was allowed to react at this temperature for 1 hr, with mixing. The temperature was then slowly raised to +120 o C, and it was kept at this height for 2 hrs.
  • the treatment was repeated with 300 ml of TiCl4 at +120 o C for 2 hrs.
  • the product was further washed with 300 ml of heptane at +70 o C. The washing was repeated five times, and the product thus obtained was dried in vacuum at room temperature.
  • the dry catalyst had violet colour
  • the analytic results of the catalyst were: Ti 2.4% by wt.: Mg 16.9% by wt., and Cl 50.5% by wt.
  • the activity of the catalyst was 334 kg polypropylene per g Ti.
  • the evaporation residue from the polymerizing fluid was 0.8% by wt., referred to the total polypropylene quantity obtained.
  • the polypropylene had isotacticity 99.2%, isotacticity index 98.6% and specific density 0.46 g/cm3.
  • the melt index of the polymer was 4.4 g/10 min.
  • the polymer that was obtained was round in shape and free-flowing.
  • the polymer had the following particle distribution:- Particle size, mm % by weight of the product > 2.0 0.1 2.0 - 1.0 79.1 1.0 - 0.5 16.7 0.5 - 0.18 2.4 0.18 - 0.10 0.8 0.10 - 0.056 0.6 ⁇ 0.056 0.3
  • the analytic results of the catalyst were: Ti 2.0% by wt., Mg 16.7% by wt., and Cl 51.3% by wt.
  • the results of polymerizing were as follows.
  • the activity of the catalyst was 345 kg polypropylene per g Ti.
  • the evaporation residue from the polymerizing fluid was 2.2% by wt. of the total quantity of polymer obtained.
  • the polymer had isotacticity 99.2%, isotacticity index 97.0% and specific gravity 0.47 g/cm3.
  • the melt index of the polymer was 7.1 g/10 min.
  • the polymer that was obtained was round in shape and free-flowing.
  • the particle size distribution of the polymer was:- particle size, mm % by weight of the product > 2.0 0.2 2.0 - 1.0 70.5 1.0 - 0.5 20.9 0.5 - 0.18 6.1 0.18 - 0.10 1.3 0.10 - 0.056 0.7 ⁇ 0.056 0.3
  • the quality characteristics of the catalyst activated by the catalyst carrier manufacturing procedure of the invention are eminently reproducible, which is a decisive factor in process catalyst manufacturing.
  • the particle size distribution of the solid product was:- Particle size, micra % by weight of total weight > 105 30.2 105 - 74 33.7 ⁇ 74 36.1
  • the analytic result was: Mg 9.6% by wt., Cl 27.8% by wt., corresponding to the composition of the input melt, MgCl2 ⁇ 3 EtOH ⁇ 0.05 DIBP.
  • the catalyst was prepared as in Example 1.
  • the analytic results of the catalyst were: Ti 3.5% by wt., Mg 13.0% by wt., and Cl 50.6% by wt.
  • the morphology of the polypropylene was spherical, but it was slightly sticky owing to low isotacticity index.
  • the particle size distribution of the polymer was:- Particle size, mm % by weight of the product > 2.0 0.1 2.0 - 1.0 65.3 1.0 - 0.5 29.0 0.5 - 0.18 4.7 0.18 - 0.10 0.5 0.10 - 0.056 0.4 ⁇ 0.056 -
  • a nitrogenated autoclave of capacity 110 litres was charged with 35 kg of dry MgCl2 and 80 litres of dry EtOH. This reaction mix was melted at 140 o C, with mixing at the ultimate stage. After mixing for 8 hrs, the clear, homogenized mixture was supplied at a rate of 10 kg/h into a cooled spray chamber, which was cooled with nitrogen at -20 o C.
  • the nozzle type was a 9-mm gas/liquid fluidizing nozzle with melt feeding aperture 1.0 mm in diameter and spraying angle 60 o . Nitrogen at 140 o C served as spraying gas, its feed rate being 1 kg/h.
  • the product was free-flowing and spherical in shape.
  • the product had the same chemical composition as the starting material melt (MgCl2 ⁇ 3.7 EtOH).
  • the particle distribution was in the range 10-300 micra.
  • the fraction ⁇ 74 micra was separated from the product by screening, for activation.
  • Example 2 Polymerizing was performed as in Example 1.
  • the activity of the catalyst was 380 kg polypropylene per g Ti.
  • the evaporation residue from the polymerizing fluid was 0.5% by wt; of the total quantity of polymer obtained.
  • the isotacticity of the polypropylene was 98.0%, isotacticity index 97.5% and specific gravity 0.40 g/cm3.
  • the particle size distribution of the polymer was:- Particle size, mm % by weight of the product > 2.0 0.10 2.0 - 1.0 43.4 1.0 - 0.5 37.9 0.5 - 0.18 15.1 0.18 - 0.10 2.2 0.10 - 0.056 1.0 ⁇ 0.056 0.3
  • the solid product had the following particle size distribution:- Particle size, micra % of total weight > 105 42.2 105 - 74 27.6 ⁇ 74 30.2
  • the analytic result was: Mg 11.1% by wt., Cl 30.2% by wt.
  • the gross formula of the complex corresponds to MgCl2 ⁇ 2.9 EtOH.
  • the product was free-flowing, spherical powder. 0.105 moles of MgCl2 ⁇ 2.9 EtOH with size ⁇ 74 micra were activated as in Example 3, with the exception that the TiCl2/EtOH mole proportion was 8.7 in the first and second titanizing. The DIBP/Mg molar proportion employed was 0.2.
  • the analytic results of the catalyst were: Ti 4.6% by wt., Mg 13.1% by wt., and Cl 52.3% by wt.
  • the catalyst was used to polymerize propylene as in Example 1.
  • the polypropylene had spherical morphology.
  • the particle size distribution of the polymer was:- Particle size, mm % by weight of the product > 2.0 0.1 2.0 - 1.0 60.9 1.0 - 0.5 35.4 0.5 - 0.18 4.0 0.18 - 0.10 0.4 0.10 - 0.056 0.2 ⁇ 0.056 -
  • a catalyst was prepared otherwise as in Example 4, but MgCl2 ⁇ 3 EtOH was used for starting material and preparation took place without diisobutylphtalate. The catalyst had yellowish-brown colour.
  • the analytic data of the catalyst were: Ti 9.2% by wt., Mg 12.8% by wt., and Cl 59.0% by wt.
  • Polymerizing was performed as in Example 1.
  • the activity of the catalyst was 75 kg PP per g Ti.
  • the evaporation residue from the polymerizing fluid was 17.4% by wt. of the total polymer quantity obtained.
  • the polypropylene had isotacticity 79.4% and isotacticity index 65.6%. Its specific density could not be determined because the solid polymer was agglomerated and it was not free-flowing.
  • the component to be sprayed was prepared as in Example 3, except that the EtOH/MgCl2 molar proportion was 8, and TiCl4 was added to the mixture applying MgCl2/TiCl2 molar proportion 1.
  • the product thus obtained was melted at +90 o C and spray-crystallized.
  • the product which was obtained had the composition: MgCl2 TiCl2 (OEt)2 ⁇ 6.0 EtOH.
  • the analytic results of the catalyst were: Ti 3.2% by wt., Mg 15.0% by wt., Cl 59.9% by wt.
  • Polymerizing was performed as in Example 1.
  • the activity of the catalyst was 70 kg PP per g Ti.
  • the evaporation residue from the polymerizing fluid was 15.1% of the total polymer quantity obtained.
  • the polypropylene presented isotacticity 95.5% and isotacticity index 81.0%. Specific density was 0.36 g/cm3.
  • a catalyst of this type is therefore not appropriate for use in polymerizing processes (e.g. polypropylene, polybutylene, poly-4-methyl-1-pentylene, etc.).

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
EP87904047A 1986-06-09 1987-06-09 Procedure for manufacturing catalyst components for polymerizing olefines Expired - Lifetime EP0279818B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI862459A FI80055C (fi) 1986-06-09 1986-06-09 Foerfarande foer framstaellning av katalytkomponenter foer polymerisation av olefiner.
FI862459 1986-06-09

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EP0279818A1 EP0279818A1 (en) 1988-08-31
EP0279818B1 true EP0279818B1 (en) 1993-04-21

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EP87904047A Expired - Lifetime EP0279818B1 (en) 1986-06-09 1987-06-09 Procedure for manufacturing catalyst components for polymerizing olefines

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US (1) US4829034A (OSRAM)
EP (1) EP0279818B1 (OSRAM)
JP (1) JPH0791330B2 (OSRAM)
AT (1) AT394855B (OSRAM)
CH (1) CH671767A5 (OSRAM)
DE (2) DE3790287C2 (OSRAM)
FI (1) FI80055C (OSRAM)
GB (1) GB2199767B (OSRAM)
NL (1) NL191263C (OSRAM)
NO (1) NO168827C (OSRAM)
SE (1) SE458927B (OSRAM)
WO (1) WO1987007620A1 (OSRAM)

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EP3543247A1 (en) * 2012-09-24 2019-09-25 INDIAN OIL CORPORATION Ltd. Precursor for catalyst, process for preparing the same and its use thereof

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JP5069414B2 (ja) 2002-12-18 2012-11-07 バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ 二塩化マグネシウムベースの付加物およびそれから得られる触媒成分
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SE458927B (sv) 1989-05-22
GB2199767B (en) 1990-08-22
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DE3790287T1 (OSRAM) 1988-06-23
FI80055C (fi) 1990-04-10
CH671767A5 (OSRAM) 1989-09-29
SE8800363D0 (sv) 1988-02-05
AT394855B (de) 1992-07-10
NL191263B (nl) 1994-11-16
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NO880350L (no) 1988-01-27
EP0279818A1 (en) 1988-08-31
US4829034A (en) 1989-05-09
FI862459A0 (fi) 1986-06-09
DE3790287C2 (de) 2001-05-03
NL191263C (nl) 1995-04-18
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ATA901687A (de) 1991-12-15
GB8801276D0 (en) 1988-03-16

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